Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g55120 | A03 | 27244753 | G | A | missense_variant | MODERATE | c.829G>A|p.Asp277Asn |
S298 |
2 | BAA03g55120 | A03 | 27246378 | C | T | splice_region_variant&intron_variant | LOW | c.1526-4C>T| |
S216 |
3 | BAA03g55120 | A03 | 27247491 | C | T | intron_variant | MODIFIER | c.2063-201C>T| |
S199 |
4 | BAA03g55120 | A03 | 27247593 | C | T | intron_variant | MODIFIER | c.2063-99C>T| |
S277 |
5 | BAA03g55120 | A03 | 27247643 | C | T | intron_variant | MODIFIER | c.2063-49C>T| |
S15 S3 |
6 | BAA03g55120 | A03 | 27248176 | C | T | synonymous_variant | LOW | c.2425C>T|p.Leu809Leu |
S172 S217 |
7 | BAA03g55120 | A03 | 27248459 | C | T | missense_variant | MODERATE | c.2708C>T|p.Ser903Phe |
S4 |
8 | BAA03g55120 | A03 | 27248486 | C | T | missense_variant | MODERATE | c.2735C>T|p.Pro912Leu |
S279 |
9 | BAA03g55120 | A03 | 27248526 | C | T | synonymous_variant | LOW | c.2775C>T|p.Arg925Arg |
S236 |
10 | BAA03g55120 | A03 | 27248985 | C | T | missense_variant | MODERATE | c.3152C>T|p.Pro1051Leu |
S200 |
11 | BAA03g55120 | A03 | 27249089 | C | T | intron_variant | MODIFIER | c.3181-14C>T| |
S79 S91 |
12 | BAA03g55120 | A03 | 27249403 | G | A | downstream_gene_variant | MODIFIER | c.*19G>A| |
S109 |
13 | BAA03g55120 | A03 | 27249416 | C | T | downstream_gene_variant | MODIFIER | c.*32C>T| |
S270 |
14 | BAA03g55120 | A03 | 27249923 | G | A | downstream_gene_variant | MODIFIER | c.*539G>A| |
S25 |
15 | BAA03g55120 | A03 | 27251421 | C | T | downstream_gene_variant | MODIFIER | c.*2037C>T| |
S250 |
16 | BAA03g55120 | A03 | 27252521 | G | A | downstream_gene_variant | MODIFIER | c.*3137G>A| |
S284 |
17 | BAA03g55120 | A03 | 27252648 | G | A | downstream_gene_variant | MODIFIER | c.*3264G>A| |
S262 |
18 | BAA03g55120 | A03 | 27252652 | C | T | downstream_gene_variant | MODIFIER | c.*3268C>T| |
S36 |
19 | BAA03g55120 | A03 | 27252741 | G | A | downstream_gene_variant | MODIFIER | c.*3357G>A| |
S95 |